JP3373590B2 - Sliding member - Google Patents

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JP3373590B2
JP3373590B2 JP13367293A JP13367293A JP3373590B2 JP 3373590 B2 JP3373590 B2 JP 3373590B2 JP 13367293 A JP13367293 A JP 13367293A JP 13367293 A JP13367293 A JP 13367293A JP 3373590 B2 JP3373590 B2 JP 3373590B2
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Japan
Prior art keywords
film
coating
sliding
wear
oxygen
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JPH06346076A (en
Inventor
ウォルフ ジョージ
政治 長谷井
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Riken Corp
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Riken Corp
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Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明は、摺動部に硬質皮膜を有
する、自動車部品やコンプレッサー部品などの機械部品
に用いられる摺動部材に関し、更に詳しく述べるなら
ば、チタンを主たる金属成分としさらに1種または2種
以上の金属元素と窒素及び酸素からなる皮膜を被覆した
摺動部材に関するものである。 【0002】 【従来の技術】自動車の内燃機関やコンプレッサーなど
の高回転化、高出力化等により機械部品などの摺動部
は、益々過酷な条件下での耐摩耗性、耐焼付性といった
摺動特性の向上が期待されている。また切削工具におい
ても切削速度増大により同様に摺動特性の向上が期待さ
れている。従来より摺動特性改善策として、硬質クロム
めっきによる耐摩耗性の改善、窒化またはモリブデン溶
射による耐焼付性の向上などの表面処理が挙げられる。 【0003】しかしながら、これらの方法では摺動材料
としての十分な摺動特性が得られず、最近物理的気相蒸
着(PVD)法あるいは化学気相析出(CVD)法によ
り化学的にも比較的安定なCr−N系、Ti−N系硬質
皮膜を作製する方法が検討されている。ところがCr−
N系皮膜は、皮膜硬度が比較的低いため、皮膜の摩耗が
起こりやすく、この点の改良は試みられているもののい
まだ十分な摺動特性は得られていない。 【0004】そこで、さらに皮膜硬さが高く、摺動特性
に優れた皮膜の開発が望まれ、Ti−N系皮膜が注目さ
れている。しかしながらTi−N系皮膜は、機械部品な
どの摺動部材として利用する場合には皮膜硬さが高すぎ
て相手材を摩耗させてしまうという欠点があり、また皮
膜と接する相手材との「初期なじみ」が悪い欠点もあ
る。ここで「初期なじみ」とは、機械加工または成膜自
体に起因する粗さをもつ摺動部材の表面が摺動開始後の
短時間の内に相手材と摺動接触し表面が微小且つ平滑に
摩耗する結果、接触面積を増加させることにより接触面
圧を低減させて、潤滑油膜切れを起こし難くし、以って
摩耗や焼き付きの発生を防ぐ性能である。Ti−N系皮
膜のような皮膜硬さの高すぎる皮膜を被覆した摺動部材
は、初期なじみが悪いことにより、摺動初期において摩
耗や焼付現象を起こしやすいという問題があった。 【0005】 【発明が解決しようとする課題】本発明は、上記の点に
鑑みて、Tiを主たる金属成分とする皮膜を被覆した摺
動材料において、耐摩耗性および耐焼付性等の摺動特性
に優れ、初期なじみが良好な硬質皮膜を被覆することに
より上記の問題を解決することを目的とする。さらに、
本出願人は上記の問題点を解決するために特願平5−1
20061号において、チタン、M群(M;クロム、バ
ナジウム、ジルコニウム、ニオブ、モリブデン、ハフニ
ウム、タンタル、タングステン及びアルミニウムから選
択された1種または2種以上の金属元素)、及び窒素か
らなり、金属元素の組成比が原子%比でM/(Ti+
M)=1〜45%である皮膜を被覆した摺動部材を提案
したが、この発明においてはさらに上記の摺動特性を改
良するとともに相手材の摩耗を少なくすることを目的と
する。 【0006】 【課題を解決するための手段】 すなわち、本発明に係
わる摺動部材は、チタン、M群(M;クロム、バナジウ
ム、ジルコニウム、ニオブ、モリブデン、ハフニウム、
タンタル及びタングステンから選択された1種または2
種以上の金属元素)、窒素及び酸素からなり、金属元素
の組成比が原子%比でM/(Ti+M)=1〜45%で
あり、かつガス元素の組成比が原子%比でO/(N+
O)=5〜80%である皮膜を基体に被覆したことを特
徴とする。この皮膜は、TiNにM群の元素及び酸素を
添加することにより、皮膜の硬さ自体はTiN皮膜より
も低いにもかかわらず、耐摩耗性及び耐焼付性並びに初
期なじみ性をTiN皮膜よりも良好にしたものである。
M群の元素及び酸素の作用について述べると、(イ)何
れもTiN皮膜の硬度を低下させるが、後者の方が硬度
低下の割合が大であり、(ロ)前者はTiN皮膜の摩擦
係数をやや増加させるものの、後者はこれを大幅に減少
させ、(ハ)何れもTiN皮膜のオイル中での腐食によ
る減量を抑制するが、前者の方が抑制程度が大である。
このような物性に対する影響でM群の元素と酸素は異な
るので、それぞれ別の群に分け、またCr,V,Zr,
Nb,Mo,Hf,Ta,Wはいずれも上記の点で共通
であるので、一つの群に含めることとした。 【0007】ここでM/(Ti+M)の金属元素組成比
が1%未満であると初期なじみ向上の効果が少なく、一
方45%を超えると耐焼付性の向上が図れないために、
金属元素組成比は1〜45%の範囲とした。ガス元素の
組成比O/(N+O)が5%未満であると相手材の摩耗
が多くなり、一方80%を越えると皮膜自体の摩耗が多
くなり摺動特性の向上は図れなかった。 【0008】基体としてはFe系、Al系、Ti系等の
各種材料を使用することができる。Ti−M−N−O系
皮膜の厚さは特に制限が無いが、1〜50μmの範囲内
であることが好ましい。同じく皮膜粗さはRaで1μm
以下であることが好ましい。 【0009】さらに、相手材としては特に制限がなく鋳
鉄もしくは鋼材、Crめっきを施したこれらの材料、溶
射皮膜付材料などが使用可能である。また、本発明の皮
膜は十分に清浄化された基体上にPVD又はCVD好ま
しくはPVDで成膜されるものである。 【0010】 【作用】TiN皮膜は初期なじみ性が悪く、一方CrN
系皮膜は耐摩耗性が悪いために、いずれも焼き付きを起
こしやすいが、Tiと他の金属元素M並びにN及びOを
共存させたTi−M−N−O系皮膜とすることにより焼
付が発生し難くなった。また初期なじみが良好になるこ
とによりなじみが実現した以降の摩耗は少なくなり、さ
らに相手材の摩耗も著しく減少した。以下、金属元素
(M)としてVを選んだ実施例により本発明を詳しく説
明する。 【0011】 【実施例】本実施例で使用した皮膜形成の基体は高クロ
ム鋼(JIS規格SUJ−2)である。基体はあらかじ
めフロン液中で超音波洗浄を行い、鏡面仕上げされた基
体表面に以下に説明する手順で陰極アークプラズマ式イ
オンプレーティングによりTi−N系硬質皮膜(比較
例)、Ti−V−N系硬質皮膜(比較例)及びTi−V
−N−O系硬質皮膜(実施例)を形成した。 【0012】超音波洗浄された基体をイオンプレーティ
ング装置の真空容器(チャンバ)内に取り付け、続いて
チャンバ内圧力が1.3×10-3Pa(パスカル)とな
るまで真空引きを行った。この真空度が達成された時点
から、チャンバ内に内蔵されているヒーターにより基体
を300〜600℃まで加熱して、基体表面に付着ある
いは吸着しているガス成分を放出させ、その後200℃
まで冷却した。 【0013】チャンバ内圧力が4×10-3Pa以下とな
った時点で、陰極とした各種組成のTi−V合金ターゲ
ットの表面でアーク放電を発生させ、TiおよびVの大
部分がイオン化された状態でターゲット表面から飛出さ
せた。 【0014】この時基体を装着した治具には−700〜
−1000Vのバイアス電圧を印加しておき、ターゲッ
トから飛び出すイオン化したTiおよびVを基体と治具
の表面に吸引し、さらにこれらのイオンを高速で被処理
面に衝突させた。このようなイオン化した金属の衝突に
より被処理面の酸化物などを削るいわゆるスパッタクリ
ーニングにより基体表面の活性化処理を行った。 【0015】その後、アーク放電が起こっているチャン
バ中に少量の窒素ガスを導入することにより一部のイオ
ン化したTiおよびVは、窒素ガスと結合し基体表面に
窒化物皮膜となって析出した。その後、さらに窒素ガス
流量を増やし所定のガス元素の組成比となる流量の酸素
ガスを導入して0.7〜4.0Pa程度の圧力とし、ま
た0〜−100Vのバイアス電圧を基体に印加して基体
表面にTi−V−N−O系硬質皮膜を1〜50μmの厚
さに形成させた。なお、比較例のTi−V−N皮膜形成
の場合は酸素ガスの導入をせずに同様に成膜を行った。
所定膜厚形成後、チャンバ内温度が150℃以下になる
まで冷却してから、膜被覆された基体をチャンバ外に取
り出した。皮膜の硬度はHv=1000〜2500の範
囲であった。 【0016】上記方法により得られた皮膜を用いて、摺
動試験を行った。 実施例2 ねずみ鋳鉄(FC25)を相手材としてピンオンディス
ク型摩擦試験機によりスカッフ試験を行った。スカッフ
試験条件は、以下の通りであった。 潤滑方法:モーターオイル#30、油温80℃、油量4
cc/sec 摩擦速度:8m/sec 接触荷重:初期2MPaから1MPaごとに焼付まで増
加させる。 摩擦時間:各荷重で180sec保持 表1にスカッフ試験結果を示す。 【0017】 【表1】 No V(Ti +V)-1 O(N +O )-1 スカッフ値 本 1 Ti−V −N −O 13 20 1.9 発 2 Ti−V −N −O 45 20 2.0 明 3 Ti−V −N −O 45 70 2.2 比 1 Ti−V −N 45 0 1.8 較 2 Ti−N 0 0 1.0 スカッフ値は、比較対象であるTi−Nを1.0とした時の値である。 【0018】本発明によるNo.1,2および3のTi
−V−N−O系皮膜は、皮膜中の金属元素に対するV原
子%(以後、単に「V原子%」と称す)がそれぞれ1
3、45および45%であり、皮膜中の窒素原子と酸素
原子の和に対する酸素原子%(以後、単に「酸素原子
%」と称する)がそれぞれ、20、20および70%で
ある。 【0019】皮膜中のV原子%と酸素原子%が皮膜の特
性に及ぼす影響を調べた。比較例としてVを含まないT
i−N系皮膜について同じ条件でスカッフ試験を行い得
られたスカッフ値(焼付面圧)1.0に対して、本発明
のNo.1、2及び3のTi−V−N−O系皮膜ではス
カッフ値が約2倍以上向上した。さらに、No.2とN
o.3のTi−V−N−O系皮膜を比較すると、酸素原
子%が大きいNo.3が高いスカッフ値を示した。 【0020】実施例3 ピン−ドラム式摩耗試験機により、ドラムにねずみ鋳鉄
(FC25)を用いて摩耗試験を行った。摩耗試験条件
は以下の通りであった。 潤滑方法:モーターオイル#30、油温80℃、油量8
cc/sec ドラム回転速度:5m/sec 接触荷重:1.5MPa 試験時間:30ksec 表2に摩耗試験結果を示す。 【0021】 【表2】 ピン ドラム No V(Ti +V)-1 O(N +O )-1 摩耗量 摩耗量 本 1 Ti−V −N −O 13 20 0.8 0.5 発 2 Ti−V −N −O 45 20 0.9 0.4 明 3 Ti−V −N −O 45 70 0.9 0.3 比 1 Ti−V −N 45 0 0.9 0.6 較 2 Ti−N 0 0 1.0 1.0 スカッフ値は、比較対象であるTi−Nを1.0とした時の値である。 【0022】比較対象として、V及び酸素を含まないT
i−N系皮膜及び酸素を含まないTi−V−N系皮膜に
ついてTi−V−N−O系皮膜と同じ条件で摩耗試験を
行った。ここで、皮膜を被覆したピンの摩耗量は摩耗し
た接触面のドラム回転方向の幅、ドラムの摩耗量はドラ
ムの摩耗深さより求めた。Ti−N系皮膜の場合のピン
摩耗量及びドラム摩耗量をそれぞれ1.0としてそれぞ
れの特性を表2に示す。 【0023】本発明によるTi−V−N−0系皮膜は、
ピン摩耗量は比較例とほぼ同程度であり、一方ドラムの
摩耗量は比較例に比べ著しく低減している。特に、V原
子%が45%、酸素原子%が70%のTi−V−N−O
系皮膜(No.3)では、Ti−N系皮膜の約1/3,
Ti−V−N系皮膜の半分近い摩耗量に抑えられてい
る。 【0024】以上のスカッフ試験および摩耗試験の結果
から、Ti−N系皮膜及びTi−V−N系皮膜に比べT
i−V−N−O系皮膜は、耐焼付性に優れ、初期なじみ
が良好で、摺動部相手材の摩耗を抑えられる皮膜である
ことがわかった。 【0025】 【発明の効果】以上のように、摺動面に主たる金属成分
であるTi,他の金属元素、窒素及び酸素からなる皮膜
を被覆することにより、相手材を摩耗させることがな
く、初期なじみが良好で、耐摩耗性および耐焼付性等の
摺動特性に優れた摺動部材が得られる。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sliding member having a hard coating on a sliding portion and used for machine parts such as automobile parts and compressor parts. Then, the present invention relates to a sliding member in which titanium is used as a main metal component and further coated with a film made of one or more metal elements and nitrogen and oxygen. 2. Description of the Related Art Sliding parts such as mechanical parts are increasingly used under increasingly severe conditions, such as abrasion resistance and seizure resistance, due to high speed and high output of internal combustion engines and compressors of automobiles. Improvements in dynamic characteristics are expected. Similarly, with respect to cutting tools, it is expected that the sliding characteristics will be improved by increasing the cutting speed. Conventionally, surface treatments such as improvement of abrasion resistance by hard chromium plating, and improvement of seizure resistance by nitridation or molybdenum spraying have been mentioned as measures for improving sliding characteristics. [0003] However, these methods do not provide sufficient sliding properties as a sliding material, and have recently been relatively chemically modified by physical vapor deposition (PVD) or chemical vapor deposition (CVD). A method for producing a stable Cr—N-based or Ti—N-based hard coating has been studied. However, Cr-
Since the N-based coating has a relatively low coating hardness, the coating is liable to wear, and although an attempt has been made to improve this point, sufficient sliding characteristics have not yet been obtained. [0004] Therefore, the development of a film having higher film hardness and excellent sliding characteristics has been desired, and a Ti-N-based film has attracted attention. However, when used as a sliding member such as a machine part, the Ti-N-based coating has a disadvantage that the coating hardness is too high and causes the mating material to be worn. There is also a drawback that "adaptation" is bad. Here, “initial adaptation” means that the surface of a sliding member having roughness due to machining or film formation itself comes into sliding contact with a counterpart material within a short time after the start of sliding, and the surface is fine and smooth. As a result, the contact surface pressure is reduced by increasing the contact area, making it difficult for the lubricating oil film to break, thereby preventing the occurrence of abrasion and seizure. A sliding member coated with a coating having an excessively high hardness, such as a Ti-N-based coating, has a problem in that wear and seizure are likely to occur in the initial stage of sliding due to poor initial adaptation. SUMMARY OF THE INVENTION In view of the above problems, the present invention provides a sliding material coated with a coating containing Ti as a main metal component, such as a sliding material having wear resistance and seizure resistance. An object of the present invention is to solve the above-mentioned problems by coating a hard film having excellent characteristics and good initial conformability. further,
The present applicant has made Japanese Patent Application No. 5-1 to solve the above problem.
No. 20061; titanium, group M (M; one or more metal elements selected from chromium, vanadium, zirconium, niobium, molybdenum, hafnium, tantalum, tungsten and aluminum), and nitrogen, Is M / (Ti +
Although a sliding member coated with a film having M) of 1 to 45% has been proposed, an object of the present invention is to further improve the above-described sliding characteristics and reduce wear of a mating material. That is, the sliding member according to the present invention is made of titanium, group M (M; chromium, vanadium, zirconium, niobium, molybdenum, hafnium,
One or two selected from tantalum and tungsten
Or more metal elements), nitrogen and oxygen, the composition ratio of the metal elements is M / (Ti + M) = 1 to 45% in atomic% ratio, and the composition ratio of the gas elements is O / ( N +
O) = 5 to 80% is coated on the substrate. This film has abrasion resistance, seizure resistance, and initial conformability that are lower than those of the TiN film, even though the hardness of the film itself is lower than that of the TiN film, by adding an element of Group M and oxygen to TiN. It was a good one.
Regarding the effects of the elements of group M and oxygen, (a) all decrease the hardness of the TiN film, but the latter has a higher rate of hardness decrease, and (b) the former has a lower coefficient of friction of the TiN film. Although slightly increased, the latter greatly reduces this. (C) In each case, the weight loss due to corrosion of the TiN film in oil is suppressed, but the former is more suppressed.
Since the elements and oxygen in the M group are different due to such influence on physical properties, they are divided into different groups, respectively, and Cr, V, Zr,
Since Nb, Mo, Hf, Ta, and W are all common in the above points, they are included in one group. Here, if the metal element composition ratio of M / (Ti + M) is less than 1%, the effect of improving the initial penetration is small, while if it exceeds 45%, the seizure resistance cannot be improved.
The metal element composition ratio was in the range of 1 to 45%. If the composition ratio O / (N + O) of the gas element is less than 5%, the wear of the mating material increases, whereas if it exceeds 80%, the wear of the coating film itself increases and the sliding characteristics cannot be improved. Various materials such as Fe-based, Al-based and Ti-based materials can be used as the substrate. The thickness of the Ti-M-N-O-based coating is not particularly limited, but is preferably in the range of 1 to 50 m. Similarly, the film roughness is 1 μm in Ra.
The following is preferred. Further, the counterpart material is not particularly limited, and it is possible to use cast iron or steel materials, Cr-plated materials thereof, materials with a thermal spray coating, and the like. Also, the coating of the present invention is formed by PVD or CVD, preferably PVD, on a sufficiently cleaned substrate. The initial conformability of the TiN film is poor.
Since the system coating has poor abrasion resistance, seizure is likely to occur in each case. However, seizure occurs when a Ti-M-N-O system film in which Ti and other metal elements M and N and O coexist. It became difficult to do. In addition, since the initial adaptation was improved, the wear after the adaptation was realized was reduced, and the wear of the mating material was also significantly reduced. Hereinafter, the present invention will be described in detail with reference to Examples in which V is selected as the metal element (M). [0011] The substrate for forming a film used in this embodiment is a high chromium steel (JIS standard SUJ-2). The substrate was subjected to ultrasonic cleaning in a fluorocarbon solution in advance, and a mirror-finished substrate surface was subjected to cathodic arc plasma ion plating by a procedure described below to form a Ti-N-based hard film (comparative example), Ti-V-N Hard Coating (Comparative Example) and Ti-V
A -NO hard coating (Example) was formed. The substrate subjected to ultrasonic cleaning was mounted in a vacuum vessel (chamber) of an ion plating apparatus, and then vacuum was drawn until the pressure in the chamber reached 1.3 × 10 −3 Pa (Pascal). When the degree of vacuum is achieved, the substrate is heated to 300 to 600 ° C. by a heater built in the chamber to release gas components attached or adsorbed on the surface of the substrate.
Cooled down. When the pressure in the chamber becomes 4 × 10 −3 Pa or less, an arc discharge is generated on the surface of a Ti—V alloy target having various compositions as a cathode, and most of Ti and V are ionized. And let it fly out of the target surface. At this time, the jig on which the base is mounted is -700 to
A bias voltage of -1000 V was applied, ionized Ti and V jumping out of the target were attracted to the surface of the substrate and the jig, and these ions collided with the surface to be processed at high speed. An activation treatment of the substrate surface was performed by so-called sputter cleaning in which oxides and the like on the surface to be treated were scraped by the collision of the ionized metal. Thereafter, by introducing a small amount of nitrogen gas into the chamber where the arc discharge is occurring, a portion of ionized Ti and V were combined with the nitrogen gas and deposited as a nitride film on the substrate surface. Thereafter, the flow rate of nitrogen gas is further increased to introduce a flow rate of oxygen gas having a composition ratio of a predetermined gas element to a pressure of about 0.7 to 4.0 Pa, and a bias voltage of 0 to -100 V is applied to the substrate. Thus, a Ti-VNO-based hard coating was formed on the surface of the substrate to a thickness of 1 to 50 µm. In the case of forming the Ti-V-N film of the comparative example, the film was formed in the same manner without introducing oxygen gas.
After the formation of the predetermined film thickness, the temperature in the chamber was cooled to 150 ° C. or less, and then the substrate covered with the film was taken out of the chamber. The hardness of the coating was in the range of Hv = 1000 to 2500. Using the coating obtained by the above method, a sliding test was performed. Example 2 A scuff test was performed using a gray cast iron (FC25) as a mating material using a pin-on-disk friction tester. The scuff test conditions were as follows. Lubrication method: motor oil # 30, oil temperature 80 ° C, oil amount 4
cc / sec Friction speed: 8 m / sec Contact load: Increase from initial 2 MPa to seizure every 1 MPa. Friction time: maintained for 180 seconds under each load Table 1 shows the scuff test results. [Table 1] No V (Ti + V) -1 O (N + O) -1 Scuff value book 1 Ti-V-N-O 13 20 1.9 Departure 2 Ti-V-N-O 45 20 2.0 Description 3 Ti-V-N-O 45 70 2.2 ratio 1 Ti-V-N 45 0 1.8 comparison 2 Ti-N 0 0 1.0 Scuff value is the value when the comparison target Ti-N is 1.0 . No. 1 according to the present invention. 1, 2 and 3 Ti
The V-N-O-based film has a V atom% (hereinafter simply referred to as "V atom%") of 1% for each metal element in the film.
3, 45 and 45%, and the oxygen atom% to the sum of the nitrogen atom and the oxygen atom in the film (hereinafter simply referred to as “oxygen atom%”) is 20, 20 and 70%, respectively. The effects of the atomic percentage of V and oxygen in the coating on the properties of the coating were examined. T without V as a comparative example
A scuff test (baking surface pressure) of 1.0 obtained by performing a scuff test under the same conditions for the i-N-based coating film was compared with the No. 1 of the present invention. The scuff values of the Ti-V-N-O-based coatings 1, 2, and 3 improved about twice or more. In addition, No. 2 and N
o. When the Ti—V—N—O based coating of No. 3 is compared, No. 3 having a large oxygen atom% 3 indicated a high scuff value. Example 3 An abrasion test was performed by using a pin-drum type abrasion tester using gray cast iron (FC25) for the drum. The wear test conditions were as follows. Lubrication method: motor oil # 30, oil temperature 80 ° C, oil amount 8
cc / sec Drum rotation speed: 5 m / sec Contact load: 1.5 MPa Test time: 30 ksec Table 2 shows the wear test results. [Table 2] Pin Drum No V (Ti + V) -1 O (N + O) -1 Abrasion Abrasion Amount 1 Ti-V-N-O 13 20 0.8 0.5 Departure 2 Ti-V-N-O 45 20 0.9 0.4 bright 3 Ti-V -N -O 45 70 0.9 0.3 ratio 1 Ti-V -N 45 0 0.9 0.6 ratio 2 Ti-N 0 0 1.0 1.0 Scuff value is 1 for Ti-N to be compared. 0.0. For comparison, V and oxygen-free T
An abrasion test was performed on the iN-based film and the Ti-VN-based film containing no oxygen under the same conditions as the Ti-VNO-based film. Here, the wear amount of the pin coated with the film was determined from the width of the worn contact surface in the drum rotation direction, and the drum wear amount was determined from the wear depth of the drum. Table 2 shows the characteristics of each of the pin-wear amount and the drum wear amount in the case of the Ti—N-based coating, assuming 1.0. The Ti-VN-0-based coating according to the present invention comprises:
The pin abrasion amount is almost the same as the comparative example, while the drum abrasion amount is significantly reduced as compared with the comparative example. In particular, Ti-V-N-O having 45% V atom% and 70% oxygen atom%
In the system-based coating (No. 3), about 1/3 of the Ti-N-based coating was used.
The amount of wear is suppressed to almost half that of the Ti-V-N-based coating. From the results of the above scuff test and abrasion test, the T-N-based film and the Ti-V-N-based film
The i-V-N-O-based film was found to be a film having excellent seizure resistance, good initial conformability, and capable of suppressing abrasion of a sliding member. As described above, by coating the sliding surface with a film composed of Ti, which is a main metal component, other metal elements, nitrogen and oxygen, the mating material is not worn out. A sliding member with good initial conformability and excellent sliding characteristics such as wear resistance and seizure resistance can be obtained.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI C10N 30:06 C10N 30:06 30:08 30:08 40:02 40:02 50:08 50:08 (56)参考文献 特開 平6−145958(JP,A) 特開 昭59−118879(JP,A) 特開 昭61−294659(JP,A) 特開 昭63−186032(JP,A) 特開 平2−88696(JP,A) 特開 平3−188261(JP,A) 特開 平2−47253(JP,A) 特開 平3−229882(JP,A) 特許3256024(JP,B2) 特公 平7−74429(JP,B2) (58)調査した分野(Int.Cl.7,DB名) C10M 103/06 C10N 10:06 - 10:12 C10N 30:06 - 30:08 C10N 40:02 C10N 50:08 F16C 33/12 C23C 14/06 - 14/08 C23C 26/00 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification code FI C10N 30:06 C10N 30:06 30:08 30:08 40:02 40:02 50:08 50:08 (56) References JP-A-6-145958 (JP, A) JP-A-59-118879 (JP, A) JP-A-61-294659 (JP, A) JP-A-63-186032 (JP, A) JP-A-2-88696 (JP-A-2-88696) JP, A) JP-A-3-188261 (JP, A) JP-A-2-47253 (JP, A) JP-A-3-229882 (JP, A) Patent 3256024 (JP, B2) JP-B-7-74429 (JP, B2) (58) Investigated field (Int. Cl. 7 , DB name) C10M 103/06 C10N 10:06-10:12 C10N 30:06-30:08 C10N 40:02 C10N 50:08 F16C 33/12 C23C 14/06-14/08 C23C 26/00

Claims (1)

(57)【特許請求の範囲】 【請求項1】 チタン、M群(M;クロム、バナジウ
ム、ジルコニウム、ニオブ、モリブデン、ハフニウム、
タンタル及びタングステンから選択された1種または2
種以上の金属元素)、窒素及び酸素からなり、金属元素
の組成比が原子%比でM/(Ti+M)=1〜45%で
あり、かつガス元素の組成比が原子%比O/(N+O)
=5〜80%である皮膜を基体に被覆したことを特徴と
する摺動部材。
(57) [Claims 1] Titanium, group M (M; chromium, vanadium, zirconium, niobium, molybdenum, hafnium,
One or two selected from tantalum and tungsten
Or more metal elements), nitrogen and oxygen, the composition ratio of the metal elements is M / (Ti + M) = 1 to 45% in atomic% ratio, and the composition ratio of the gas elements is atomic ratio O / (N + O). )
= 5% to 80% of the base member coated with a coating.
JP13367293A 1993-06-03 1993-06-03 Sliding member Expired - Fee Related JP3373590B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13367293A JP3373590B2 (en) 1993-06-03 1993-06-03 Sliding member

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Application Number Priority Date Filing Date Title
JP13367293A JP3373590B2 (en) 1993-06-03 1993-06-03 Sliding member

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JP3373590B2 true JP3373590B2 (en) 2003-02-04

Family

ID=15110208

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8245407B2 (en) 2001-11-13 2012-08-21 Acme United Corporation Coating for cutting implements
EP2980265A4 (en) * 2013-03-28 2016-11-30 Osg Corp Hard film for machining tools and hard film-coated metal machining tool

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001032064A (en) * 1999-07-23 2001-02-06 Nippon Sheet Glass Co Ltd Production of substrate for display and substrate for display produced by the producing method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8245407B2 (en) 2001-11-13 2012-08-21 Acme United Corporation Coating for cutting implements
EP2980265A4 (en) * 2013-03-28 2016-11-30 Osg Corp Hard film for machining tools and hard film-coated metal machining tool
US9551062B2 (en) 2013-03-28 2017-01-24 Osg Corporation Hard film for machining tools and hard film-coated metal machining tool

Also Published As

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JPH06346076A (en) 1994-12-20

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